GB1362437A - Process for producing penicilin derivatives - Google Patents

Abstract

1362437 Preparing penicillin esters TOYAMA CHEMICAL CO Ltd 23 June 1972 [8 July 1971] 29537/72 Heading C2A Esters of 6-acylaminopenicillanic acids and their 1-sulphoxides are prepared by reacting a salt of the said penicillanic acid or 1-sulphoxide with an imino ether salt obtained by reacting an N,N-disubstituted acid amide of Formula (I) in which R<SP>1</SP> is hydrogen or a substituted or unsubstituted alkyl, aryl, aralkyl or cycloalkyl group, and each of R<SP>2</SP> and R<SP>3</SP> is an alkyl group or R<SP>2</SP> and R<SP>3</SP> together with the common nitrogen atom form a pyrrolidine, piperidine or morpholine ring; with a chloroformate of Formula (II) in which R is -CH 2 CH 2 X, -CH 2 CHX 2 , -CH 2 CX 3 (wherein X is halogen), a succinimidomethyl group or a phthalimidomethyl group. Suitable penicillanic acid (and 1-sulphoxide) salts are the Na, K, Mg, Ca, triethyl- or tributyl - amine, N - methylmorpholine, N - ethylpiperidine, pyridine, picoline, colidine and lutidine salts of penicillin G and V and their sulphoxides and of 6-acylaminopenicillanic acids and sulphoxides thereof wherein the acyl group is thienylacetyl or phenylacetyl or the corresponding α-amino substituted group. The imino ether salt, which is not isolated, has the Formula (III) being the product of a decarboxylation reaction between the compounds (I) and (II). Preferred acid amides (I) are N,N-dimethylformamide, N,N-dimethylacetamide and N,N,-diethylformamide. The chloroformate (II) is obtained by reacting a corresponding alcohol with phosgene in the presence of an acid-binding agent. Compounds (I) and (II) are suitably reacted in amounts of from 2 to 5 moles and 1 to 1À5 moles respectively, for each mole of the penicillin in the subsequent ester-forming reaction. The penicillins can be converted to the corresponding 1-sulphoxides before or after the esterification reaction by a conventional S-oxidation procedure, e.g. with peracetic acid.